Antioxidant activity and protective role on protein glycation of synthetic aminocoumarins

Background: Synthesized aminocoumarins are heterocyclic compounds possessing potential for the treatment of insulin-dependent diabetes mellitus with unexplored anti-glycative action. Results: In this study 4-aminocoumarin derivatives (4-ACDs) were evaluated in vitro for antiglycation (AG) activities...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Aminjafari,Akram, Miroliaei,Mehran, Angelova,Violina T, Emamzadeh,Rahman, Djukic,Mirjana M, Djuric,Ana, Saso,Luciano
Lenguaje:English
Publicado: Pontificia Universidad Católica de Valparaíso 2016
Materias:
Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582016000600007
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:scielo:S0717-34582016000600007
record_format dspace
spelling oai:scielo:S0717-345820160006000072017-01-25Antioxidant activity and protective role on protein glycation of synthetic aminocoumarinsAminjafari,AkramMiroliaei,MehranAngelova,Violina TEmamzadeh,RahmanDjukic,Mirjana MDjuric,AnaSaso,Luciano Anti-glycation agents Diabetes, 4-Aminocoumarin derivatives Congo red Spectropolarimetry Spectrofluorimetry Background: Synthesized aminocoumarins are heterocyclic compounds possessing potential for the treatment of insulin-dependent diabetes mellitus with unexplored anti-glycative action. Results: In this study 4-aminocoumarin derivatives (4-ACDs) were evaluated in vitro for antiglycation (AG) activities by using the human serum albumin (HSA)/glucose system, for 8 weeks of incubation. The glycation and conformational alteration of HSA in the presence of the tested compounds were evaluated by Congo red assay, fluorescence and circular dichroism spectroscopy. The antioxidant (AO) capacity were also tested by four different assays including: DPPH (2,2'-diphenyl-1-picrylhydrazyl radical), ABTS (2,2-azinobis (3-ethylbenzothiazoline-6-sulphonate) diammonium salt), FRAP (ferric reducing antioxidant power) and β-carotene-linoleic acid assay. The tested compounds showed AG and AO effects. The intensity of the accomplished AO potential is related to the type of the used assay. Significant alterations in the secondary (monitored by CD spectropolarimetry) and tertiary structure (assessed by spectrofluorimetry) of HSA upon glycation were mitigated by the 4-ACDs, suggesting their suppressive role in the late stage (post-Amadori) of the HSA glycation. Conclusions: By the analogues, in vitro ascertained AO and AG properties of 4-ACD may be recognized as rationale for their protective role against oxidative changes of proteins, thereby precluding diabetic complications in humans.info:eu-repo/semantics/openAccessPontificia Universidad Católica de ValparaísoElectronic Journal of Biotechnology v.19 n.6 20162016-11-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582016000600007en10.1016/j.ejbt.2016.08.004
institution Scielo Chile
collection Scielo Chile
language English
topic Anti-glycation agents
Diabetes, 4-Aminocoumarin derivatives
Congo red
Spectropolarimetry
Spectrofluorimetry
spellingShingle Anti-glycation agents
Diabetes, 4-Aminocoumarin derivatives
Congo red
Spectropolarimetry
Spectrofluorimetry
Aminjafari,Akram
Miroliaei,Mehran
Angelova,Violina T
Emamzadeh,Rahman
Djukic,Mirjana M
Djuric,Ana
Saso,Luciano
Antioxidant activity and protective role on protein glycation of synthetic aminocoumarins
description Background: Synthesized aminocoumarins are heterocyclic compounds possessing potential for the treatment of insulin-dependent diabetes mellitus with unexplored anti-glycative action. Results: In this study 4-aminocoumarin derivatives (4-ACDs) were evaluated in vitro for antiglycation (AG) activities by using the human serum albumin (HSA)/glucose system, for 8 weeks of incubation. The glycation and conformational alteration of HSA in the presence of the tested compounds were evaluated by Congo red assay, fluorescence and circular dichroism spectroscopy. The antioxidant (AO) capacity were also tested by four different assays including: DPPH (2,2'-diphenyl-1-picrylhydrazyl radical), ABTS (2,2-azinobis (3-ethylbenzothiazoline-6-sulphonate) diammonium salt), FRAP (ferric reducing antioxidant power) and β-carotene-linoleic acid assay. The tested compounds showed AG and AO effects. The intensity of the accomplished AO potential is related to the type of the used assay. Significant alterations in the secondary (monitored by CD spectropolarimetry) and tertiary structure (assessed by spectrofluorimetry) of HSA upon glycation were mitigated by the 4-ACDs, suggesting their suppressive role in the late stage (post-Amadori) of the HSA glycation. Conclusions: By the analogues, in vitro ascertained AO and AG properties of 4-ACD may be recognized as rationale for their protective role against oxidative changes of proteins, thereby precluding diabetic complications in humans.
author Aminjafari,Akram
Miroliaei,Mehran
Angelova,Violina T
Emamzadeh,Rahman
Djukic,Mirjana M
Djuric,Ana
Saso,Luciano
author_facet Aminjafari,Akram
Miroliaei,Mehran
Angelova,Violina T
Emamzadeh,Rahman
Djukic,Mirjana M
Djuric,Ana
Saso,Luciano
author_sort Aminjafari,Akram
title Antioxidant activity and protective role on protein glycation of synthetic aminocoumarins
title_short Antioxidant activity and protective role on protein glycation of synthetic aminocoumarins
title_full Antioxidant activity and protective role on protein glycation of synthetic aminocoumarins
title_fullStr Antioxidant activity and protective role on protein glycation of synthetic aminocoumarins
title_full_unstemmed Antioxidant activity and protective role on protein glycation of synthetic aminocoumarins
title_sort antioxidant activity and protective role on protein glycation of synthetic aminocoumarins
publisher Pontificia Universidad Católica de Valparaíso
publishDate 2016
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582016000600007
work_keys_str_mv AT aminjafariakram antioxidantactivityandprotectiveroleonproteinglycationofsyntheticaminocoumarins
AT miroliaeimehran antioxidantactivityandprotectiveroleonproteinglycationofsyntheticaminocoumarins
AT angelovaviolinat antioxidantactivityandprotectiveroleonproteinglycationofsyntheticaminocoumarins
AT emamzadehrahman antioxidantactivityandprotectiveroleonproteinglycationofsyntheticaminocoumarins
AT djukicmirjanam antioxidantactivityandprotectiveroleonproteinglycationofsyntheticaminocoumarins
AT djuricana antioxidantactivityandprotectiveroleonproteinglycationofsyntheticaminocoumarins
AT sasoluciano antioxidantactivityandprotectiveroleonproteinglycationofsyntheticaminocoumarins
_version_ 1718441938092294144